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Data sharing to improve concordance in variant interpretation across laboratories: results from the Canadian Open Genetics Repository

by Mighton, Chloe, Smith, Amanda C, Mayers, Justin, Tomaszewski, Robert, Taylor, Sherryl, Hume, Stacey, Agatep, Ron, Spriggs, Elizabeth, Feilotter, Harriet E, Semenuk, Laura, Wong, Henry, Silver, Talia, Charames, George S, Di Gioacchino, Vanessa, Watkins, Nicholas, Foulkes, William D, Clavier, Marcos, Hamel, Nancy, Chong, George, Lamont, Ryan E, Parboosingh, Jillian, Young, Sean S, Akbari, Mohammad Reza, Speevak, Marsha D, Lebo, Matthew S, Agatep, Ron, Ainsworth, Peter, Akbari, Mohammad R., Aronson, Melyssa, Basran, Raveen, Blumenthal, Andrea, Bombard, Yvonne, Buckley, Kathleen, Campbell, Jodi, Care, Melanie, Carson, Nancy, Chang, Martin C., Carter, Ronald, Charames, George, Chitayat, David, Chong, George, Chouinard, Edmond, Craddock, Kenneth J., Docking, Rod, Eisen, Andrea, Faghfoury, Hanna, Farrell, Sandra, Feilotter, Harriet, Fernandez, Bridget, Fiume, Marc, Friedman, Jan, Foulkes, William, Goodhand, Peter, Hegele, Robert, Holter, Spring, Horsburgh, Sheri, Hughes, Lauren, Hume, Stacey, Jarinova, Olga, Junker, Anne, Karsan, Aly, Khalouei, Sam, Kim, Raymond H., Knoppers, Bartha, Lamont, Ryan, Lebo, Matthew, Lerner-Ellis, Jordan, Maire, Georges, Mitchell, Grant, Morel, Chantal, Nelson, Tanya, Noor, Abdul, O’Rielly, Darren, Ouellette, Francis, Parboosingh, Jillian, Rehm, Heidi, Riddell, Christie, Riviere, Jean-Baptiste, Rosenblatt, David S., Rouleau, Guy, Ruchon, Andrea, Sabatini, Peter, Sadikovic, Bekim, Semotiuk, Kara, Scherer, Stephen W., Shuman, Cheryl, Silver, Josh, Solomon-Izsak, Lesley, Speevak, Marsha, Taylor, Sherryl, Terespolsky, Deborah, Tomaszewski, Robert, Wong, Nora, Wang, Marina, Watkins, Nicholas, Waye, John S., White, Shana, Woods, Michael O., Young, Sean, Zakoor, Kathleen-Rose
Published in Journal of medical genetics (01.06.2022)

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